Variant report

Variant	rs1614641
Chromosome Location	chr7:138279083-138279084
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:138277757..138279583-chr7:138282774..138285734,2	K562	blood:
2	chr7:138272442..138274593-chr7:138278540..138281503,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1116324	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12666310	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1371463	1.00[CEU][hapmap];0.81[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1616318	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1659830	0.95[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1659831	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1659832	0.95[CEU][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1673203	0.85[JPT][hapmap]
rs1673204	0.89[CEU][hapmap];0.85[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1673206	0.95[CEU][hapmap];0.82[CHB][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1673207	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1673211	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17364560	0.90[CEU][hapmap];0.81[JPT][hapmap];0.82[AMR][1000 genomes]
rs17461551	0.90[CEU][hapmap];0.81[JPT][hapmap]
rs2353354	0.94[CEU][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3807157	0.90[CEU][hapmap];0.80[JPT][hapmap]
rs62485263	0.83[EUR][1000 genomes]
rs62485264	0.84[EUR][1000 genomes]
rs6963539	0.85[CEU][hapmap];0.81[JPT][hapmap]
rs728092	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs749546	0.89[CEU][hapmap]
rs9791462	0.83[CEU][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030956	chr7:138163169-138579519	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138272600-138280400	Weak transcription	Thymus	Thymus
2	chr7:138272600-138286200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:138273000-138284000	Weak transcription	Fetal Kidney	kidney
4	chr7:138273000-138285000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:138273000-138286200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr7:138273000-138286200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:138273600-138286800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:138278400-138279200	Enhancers	Fetal Intestine Large	intestine

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